• Senior Combination Product Technology…

    BD (Becton, Dickinson and Company) (Temecula, CA)
    …years of experience with a Bachelor's degree + Relevant experience related to combination product or medical device development and/or testing + Ability to ... of the BD/ZebraSci Combination Product Services team, the Combination Product Technology Development/ Device Engineer will assist with technical and… more
    BD (Becton, Dickinson and Company) (07/18/25)
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  • Principal Device Development Engineer…

    Regeneron Pharmaceuticals (East Greenbush, NY)
    …of an off the shelf, or an internally designed platform medical device delivery system. + Defines detailed product requirements and specifications with ... + Or equivalent combination of education and experience Previous experience in combination product / medical device development or similar area is required.… more
    Regeneron Pharmaceuticals (06/11/25)
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  • Associate Director, Device Clinical…

    Takeda Pharmaceuticals (Lexington, MA)
    …degree with 15+ years of experience** + Minimum 5 years of combination product , medical device , or pharmaceutical industry experience + Experience ... the best of my knowledge. **Job Description** **About the Role:** The Associate Director of Device Clinical Development (DCD) in the Drug Product and Device more
    Takeda Pharmaceuticals (06/06/25)
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  • Device Development Associate Principal…

    Merck (Rahway, NJ)
    …injection._ **Job description** This position will be responsible for leading and implementing medical device and combination product design controls for ... years related experience + Experience with the development drug- device combination product or a medical device component of a combination product +… more
    Merck (07/31/25)
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  • Medical Device Program Manager

    US Tech Solutions (San Bruno, CA)
    …production and align with Quality System procedures, utilizing expertise in the medical device product development life-cycle, Risk Management, ... + Managing cross-functional or cross-team projects to bring regulated medical device products to market. + Ensuring product specifications… more
    US Tech Solutions (07/18/25)
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  • Product Surveillance Tech I…

    US Tech Solutions (North Chicago, IL)
    …according to procedures. + Assess incoming documentation, including clinical forms and medical information, for complaint data and ascertain compliance to product ... specification and/or intended use as indicated in the product labeling. + Evaluate internal and external lab analysis. + Coordinate with inter- and… more
    US Tech Solutions (07/18/25)
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  • Mechanical Engineer- R&D, Medical

    Eliassen Group (Marlborough, MA)
    …development of components, subsystems and systems. . Create design documentation to support medical device product development in alignment with regulatory ... **Mechanical Engineer- R&D, Medical Device ** **Marlborough, MA** **Type:** Contract...and specifications to ensure alignment with user needs and product goals. . Develop test plans, procedures, and protocols… more
    Eliassen Group (07/25/25)
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  • Digital Device Quality Engineering Lead

    Sanofi Group (Cambridge, MA)
    …relevant field, such as engineering or life sciences. + 4+ years' experience in medical device product development (Design Control) focused on quality ... Our team has released an FDA certified class II medical device titration application. We are gearing...in design reviews + Provide Quality impact assessment for product changes + Provide quality input into CAPA and… more
    Sanofi Group (05/15/25)
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  • Product Steward

    Lilly (Indianapolis, IN)
    …discreet manufacturing and/or high speed assembly operations) + Knowledge of drug product and medical device regulatory requirements (especially cGMP, ... life better for people around the world. The IDM Product Steward is responsible for the global product...design, specifications, materials, and technical agendas for a Lilly device (s) and for providing technical support to global … more
    Lilly (07/01/25)
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  • GRA Device Lead (Director)

    Sanofi Group (Morristown, NJ)
    …The GRA Device team is a globally diverse team supporting the medical device , combination product , digital health and in-vitro diagnostic products ... BS with 10 years regulatory experience. At least 5 years of relevant medical device and/or combination product regulatory experience required. + At least 10… more
    Sanofi Group (07/15/25)
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